Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539311Generated: November 1, 2026

Water → 3-(Bromomethyl)-2-fluorobenzonitrile

https://huagongshe.com/reaction/539311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-3-methylbenzonitrileHCID 23160359—
CatalystBenzoyl PeroxideHCID 7187—
SolventAcetonitrileHCID 6342—
Product3-(Bromomethyl)-2-fluorobenzonitrileHCID 6667846570.2%

Reaction Steps

NBS (1.729 g, 9.71 mmol) was added to a solution of 2-fluoro-3-methylbenzonitrile (1.25 g, 9.25 mmol) in acetonitrile (25 mL). The obtained mixture was refluxed, and then benzoic peroxyanhydride (0.045 g, 0.18 mmol) was added. The reaction mixture was refluxed overnight, then cooled to r.t. and water was added. The aqueous phase was discarded and the organic phase was dried over MgSO4 and concentrated. The crude product was purified by flash chromatography using a gradient of EtOAc in heptane as eluent to give the title compound (1.39 g, 70% yield): 1H NMR (500 MHz, DMSO-d6) δ ppm 4.75 (s, 2 H) 7.43 (t, 1 H) 7.93 (t, 2 H); MS (EI) m/z 213 M+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865911B2
Source datasetuspto-grants-2014_10
ORD IDord-09034a4e7e1e4757b50e413998ec2978
Source noteuspto-grants-2014_10